A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9491



Internal ID15193137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:52289969..52477472hg38UCSC Ensembl
Outerchr13:52864104..53051607hg19UCSC Ensembl
Outerchr13:51762105..51949608hg18UCSC Ensembl
Outerchr13:51762105..51949608hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38187504
hg19187504
hg18187504
hg17187504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7242
Supporting Variants
SamplesNA18507
Known GenesCKAP2, THSD1, VPS36
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9491
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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